SCA8 Repeat Expansion: Large CTA/CTG Repeat Alleles Are More Common in Ataxic Patients, Including Those with SCA6

This publication has 22 references indexed in Scilit:

• Loss of the Muscle-Specific Chloride Channel in Type 1 Myotonic Dystrophy Due to Misregulated Alternative Splicing
  Molecular Cell, 2002
• Expanded CUG Repeats Trigger Aberrant Splicing of ClC-1 Chloride Channel Pre-mRNA and Hyperexcitability of Skeletal Muscle in Myotonic Dystrophy
  Molecular Cell, 2002
• A Decade of Molecular Studies of Fragile X Syndrome
  Annual Review of Neuroscience, 2002
• Genetic Testing in Spinocerebellar Ataxias
  Archives of Neurology, 2001
• High Germinal Instability of the (CTG)n at the SCA8 Locus of Both Expanded and Normal Alleles
  The American Journal of Human Genetics, 2000
• An Unstable Trinucleotide-Repeat Region on Chromosome 13 Implicated in Spinocerebellar Ataxia: A Common Expansion Locus
  The American Journal of Human Genetics, 2000
• Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia
  Nature Genetics, 2000
• Are (CTG)n expansions at the SCA8 locus rare polymorphisms?
  Nature Genetics, 2000
• The DMPK Gene of Severely Affected Myotonic Dystrophy Patients Is Hypermethylated Proximal to the Largely Expanded CTG Repeat
  The American Journal of Human Genetics, 1998
• Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel
  Nature Genetics, 1997